Polycomb repressive complex 1 provides a molecular explanation for repeat copy number dependency in FSHD muscular dystrophy.

Casa, Valentina; Runfola, Valeria; Micheloni, Stefano; Aziz, Arif; Dilworth, F Jeffrey; Gabellini, Davide

Casa, Valentina; Runfola, Valeria; Micheloni, Stefano; Aziz, Arif; Dilworth, F Jeffrey; Gabellini, Davide.

Affiliation

Casa V; Gene Expression and Muscular Dystrophy Unit, Division of Regenerative Medicine, IRCCS San Raffaele Scientific Institute, Milan 20132, Italy.
Runfola V; Università Vita-Salute San Raffaele, Milan 20132, Italy.
Micheloni S; Gene Expression and Muscular Dystrophy Unit, Division of Regenerative Medicine, IRCCS San Raffaele Scientific Institute, Milan 20132, Italy.
Aziz A; Gene Expression and Muscular Dystrophy Unit, Division of Regenerative Medicine, IRCCS San Raffaele Scientific Institute, Milan 20132, Italy.
Dilworth FJ; The Sprott Center for Stem Cell Research, Regenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, ON K1Y 4E9, Canada.
Gabellini D; The Sprott Center for Stem Cell Research, Regenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, ON K1Y 4E9, Canada.

Hum Mol Genet ; 26(4): 753-767, 2017 02 15.

Article in En | MEDLINE | ID: mdl-28040729

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Homeodomain Proteins / Microsatellite Repeats / Muscular Dystrophy, Facioscapulohumeral / DNA Copy Number Variations / Polycomb Repressive Complex 1 Limits: Humans Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2017 Document type: Article Affiliation country: Italia

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